Item request has been placed! ×
Item request cannot be made. ×
loading  Processing Request

IFITM proteins are incorporated onto HIV-1 virion particles and negatively imprint their infectivity

Item request has been placed! ×
Item request cannot be made. ×
loading   Processing Request
  • معلومة اضافية
    • Contributors:
      Interaction hôte pathogène lors de l'infection lentivirale – Host-Pathogen Interaction during Lentiviral Infection CIRI (LP2L); Centre International de Recherche en Infectiologie (CIRI); École normale supérieure de Lyon (ENS de Lyon); Université de Lyon-Université de Lyon-Université Claude Bernard Lyon 1 (UCBL); Université de Lyon-Université Jean Monnet - Saint-Étienne (UJM)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-École normale supérieure de Lyon (ENS de Lyon); Université de Lyon-Université Jean Monnet - Saint-Étienne (UJM)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS); SFR Biosciences; Université de Lyon-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS); Plateforme des Microscopies; Université de Tours (UT); Centre Hospitalier Régional Universitaire de Tours (CHRU Tours); Oncogenèse rétrovirale – Retroviral Oncogenesis CIRI (OR); Morphogénèse et antigénicité du VIH, des Virus des Hépatites et Emergents (MAVIVHe); Université de Tours (UT)-Institut National de la Santé et de la Recherche Médicale (INSERM); King‘s College London
    • بيانات النشر:
      HAL CCSD
      BioMed Central
    • الموضوع:
      2014
    • Collection:
      Université François-Rabelais de Tours: HAL
    • نبذة مختصرة :
      International audience ; BACKGROUND: Interferon induced transmembrane proteins 1, 2 and 3 (IFITMs) belong to a family of highly related antiviral factors that have been shown to interfere with a large spectrum of viruses including Filoviruses, Coronaviruses, Influenza virus, Dengue virus and HIV-1. In all these cases, the reported mechanism of antiviral inhibition indicates that the pool of IFITM proteins present in target cells blocks incoming viral particles in endosomal vesicles where they are subsequently degraded.RESULTS: In this study, we describe an additional mechanism through which IFITMs block HIV-1. In virus-producing cells, IFITMs coalesce with forming virions and are incorporated into viral particles. Expression of IFITMs during virion assembly leads to the production of virion particles of decreased infectivity that are mostly affected during entry in target cells. This mechanism of inhibition is exerted against different retroviruses and does not seem to be dependent on the type of Envelope present on retroviral particles.CONCLUSIONS: The results described here identify a novel mechanism through which IFITMs affect HIV-1 infectivity during the late phases of the viral life cycle. Put in the context of data obtained by other laboratories, these results indicate that IFITMs can target HIV at two distinct moments of its life cycle, in target cells as well as in virus-producing cells. These results raise the possibility that IFITMs could similarly affect distinct steps of the life cycle of a number of other viruses.
    • Relation:
      info:eu-repo/semantics/altIdentifier/pmid/25422070; PUBMED: 25422070; PUBMEDCENTRAL: PMC4251951
    • الرقم المعرف:
      10.1186/s12977-014-0103-y
    • الدخول الالكتروني :
      https://hal.science/hal-02322616
      https://hal.science/hal-02322616v1/document
      https://hal.science/hal-02322616v1/file/main.pdf
      https://doi.org/10.1186/s12977-014-0103-y
    • Rights:
      info:eu-repo/semantics/OpenAccess
    • الرقم المعرف:
      edsbas.C9460BD8